Author: Sarmadi, Morteza; Behrens, Adam M; McHugh, Kevin J; Contreras, Hannah T M; Tochka, Zachary L; Lu, Xueguang; Langer, Robert; Jaklenec, Ana
                    Title: Modeling, design, and machine learning-based framework for optimal injectability of microparticle-based drug formulations.  Cord-id: cgdzni2s  Document date: 2020_7_1
                    ID: cgdzni2s
                    
                    Snippet: Inefficient injection of microparticles through conventional hypodermic needles can impose serious challenges on clinical translation of biopharmaceutical drugs and microparticle-based drug formulations. This study aims to determine the important factors affecting microparticle injectability and establish a predictive framework using computational fluid dynamics, design of experiments, and machine learning. A numerical multiphysics model was developed to examine microparticle flow and needle blo
                    
                    
                    
                     
                    
                    
                    
                    
                        
                            
                                Document: Inefficient injection of microparticles through conventional hypodermic needles can impose serious challenges on clinical translation of biopharmaceutical drugs and microparticle-based drug formulations. This study aims to determine the important factors affecting microparticle injectability and establish a predictive framework using computational fluid dynamics, design of experiments, and machine learning. A numerical multiphysics model was developed to examine microparticle flow and needle blockage in a syringe-needle system. Using experimental data, a simple empirical mathematical model was introduced. Results from injection experiments were subsequently incorporated into an artificial neural network to establish a predictive framework for injectability. Last, simulations and experimental results contributed to the design of a syringe that maximizes injectability in vitro and in vivo. The custom injection system enabled a sixfold increase in injectability of large microparticles compared to a commercial syringe. This study highlights the importance of the proposed framework for optimal injection of microparticle-based drugs by parenteral routes.
 
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